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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446941Generated: October 29, 2026

Dimethylamine, hydrochloride → HCID 28165234, compound

https://huagongshe.com/reaction/446941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantDiisopropylethylamineHCID 81531—
ReactantBOC-D-alanineHCID 637606—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 28165234HCID 28165234101.2%

Reaction Steps

(R)-2-(tert-Butoxycarbonylamino)propanoic acid (1.0 g, 5.3 mmol) and O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium tetrafluoroborate (1.8 g, 5.6 mmol) were dissolved in 13 mL of dichloromethane. Dimethylamine hydrochloride (0.64 g, 7.8 mmol) and N,N-diisopropylethylamine (3.6 mL, 20.8 mmol) were added and the mixture was stirred at room temperature for 16 h. The reaction mixture was diluted with dichloromethane and water was added. The layers were separated and the aqueous layer was extracted once more with dichloromethane. The combined organic layers were washed with sodium chloride solution, dried over sodium sulfate and concentrated. The residue was purified by silica gel chromatography (ethyl acetate/hexanes) to give 1.16 g (100%) of ((R)-1-dimethylcarbamoyl-ethyl)-carbamic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481541B2
Source datasetuspto-grants-2013_07
ORD IDord-c23c30bb05c146949167ac7849a32ebc
Source noteuspto-grants-2013_07